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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 716296Generated: October 26, 2026

Acetone → Ethyl 2-((propan-2-yl)amino)acetate

https://huagongshe.com/reaction/716296

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantSodium HydroxideHCID 14798—
ReactantGlycine ethyl ester, hydrochlorideHCID 2723640—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductEthyl 2-((propan-2-yl)amino)acetateHCID 35162585%

Reaction Steps

To a suspension of ethyl 2-aminoacetate hydrochloride (20 g, 143.28 mmol) in THF (400 mL) was added glacial acetic acid (20 mL) followed by acetone (11.59 mL, 151.62 mmol). The reaction was stirred 30 min at room temperature. Sodium triacetoxyborohydride (60.73 g, 286.56 mmol) was added over the course of one hour. The reaction was poured slowly into a vigorously stirred biphasic mixture of water (300 mL) and ethyl acetate (800 mL). The aqueous layer was adjusted to pH 13 using a solution of 50% (weight) NaOH. The mixture was stirred 30 min and poured into a separatory funnel. The organic layer was collected and the aqueous layer was back extracted with ethyl acetate (3×200 mL). The organic layers were combined, washed with brine (300 mL), dried with sodium sulfate, and concentrated to yield the title compound (17.6 g, 85%) as a translucent oil which was used in the next step without further purification. [M+H] calc'd for C7H15NO2, 146. found, 146.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187497B2
Source datasetuspto-grants-2015_11
ORD IDord-8aa297fada614315ac17fdf39e9d0a71
Source noteuspto-grants-2015_11